Libersou Sonia, Siebert Xavier, Ouldali Malika, Estrozi Leandro F, Navaza Jorge, Charpilienne Annie, Garnier Pascale, Poncet Didier, Lepault Jean
Laboratoire de Virologie Moléculaire et Structurale, CNRS, UMR 2472, IFR 115, INRA, UMR 1157, 1 Avenue de la Terrasse, F-91198 Gif-sur-Yvette, France.
J Virol. 2008 Mar;82(6):2844-52. doi: 10.1128/JVI.02268-07. Epub 2008 Jan 9.
Rotaviruses are prototypical double-stranded RNA viruses whose triple-layered icosahedral capsid constitutes transcriptional machinery activated by the release of the external layer. To understand the molecular basis of this activation, we studied the structural interplay between the three capsid layers by electron cryo-microscopy and digital image processing. Two viral particles and four virus-like particles containing various combinations of inner (VP2)-, middle (VP6)-, and outer (VP7)-layer proteins were studied. We observed that the absence of the VP2 layer increases the particle diameter and changes the type of quasi-equivalent icosahedral symmetry, as described by the shift in triangulation number (T) of the VP6 layer (from T = 13 to T = 19 or more). By fitting X-ray models of VP6 into each reconstruction, we determined the quasi-atomic structures of the middle layers. These models showed that the VP6 lattices, i.e., curvature and trimer contacts, are characteristic of the particle composition. The different functional states of VP6 thus appear as being characterized by trimers having similar conformations but establishing different intertrimeric contacts. Remarkably, the external protein VP7 reorients the VP6 trimers located around the fivefold axes of the icosahedral capsid, thereby shrinking the channel through which mRNA exits the transcribing rotavirus particle. We conclude that the constraints arising from the different geometries imposed by the external and internal layers of the rotavirus capsid constitute a potential switch regulating the transcription activity of the viral particles.
轮状病毒是典型的双链RNA病毒,其三层二十面体衣壳构成了由外层释放激活的转录机制。为了理解这种激活的分子基础,我们通过电子冷冻显微镜和数字图像处理研究了衣壳三层之间的结构相互作用。研究了两种病毒颗粒和四种包含内(VP2)、中(VP6)、外(VP7)层蛋白不同组合的病毒样颗粒。我们观察到,VP2层的缺失会增加颗粒直径并改变准等效二十面体对称性的类型,如VP6层三角剖分数(T)的变化所示(从T = 13变为T = 19或更高)。通过将VP6的X射线模型拟合到每个重建结构中,我们确定了中间层的准原子结构。这些模型表明,VP6晶格,即曲率和三聚体接触,是颗粒组成的特征。因此,VP6的不同功能状态似乎以具有相似构象但建立不同三聚体间接触的三聚体为特征。值得注意的是,外部蛋白VP7会使位于二十面体衣壳五重轴周围的VP6三聚体重定向,从而缩小mRNA离开转录轮状病毒颗粒的通道。我们得出结论,轮状病毒衣壳外层和内层施加的不同几何形状所产生的限制构成了调节病毒颗粒转录活性的潜在开关。